posterior fossa cyst Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A discrete posterior fossa cerebrospinal fluid (CSF) collection that does not communicate directly with the fourth ventricle. (Human Phenotype Ontology, HP_0007291)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007291
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Genes

7 genes associated with the posterior fossa cyst phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABAT 4-aminobutyrate aminotransferase
CSPP1 centrosome and spindle pole associated protein 1
FGFR2 fibroblast growth factor receptor 2
GDF6 growth differentiation factor 6
KIAA0196 KIAA0196
POMT1 protein-O-mannosyltransferase 1
VSX1 visual system homeobox 1